List of variants reported as benign for Glycogen storage disease type X by Illumina Laboratory Services, Illumina

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000290.4(PGAM2):c.324G>A (p.Gly108=)	rs112828964	0.02943
NM_000290.4(PGAM2):c.341T>G (p.Ile114Ser)	rs61756062	0.02444
NM_000290.4(PGAM2):c.216C>T (p.Asp72=)	rs111656877	0.01481
NM_000290.4(PGAM2):c.290G>A (p.Gly97Asp)	rs77938727	0.00026

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